O-Methylhydroxylamine hydrochloride → HCID 131736105, compound
Reaction equation
[Cl:1][C:2]1[CH:3]=[C:4]2[C:8](=[C:9]([Cl:11])[CH:10]=1)[C:7](=O)[CH2:6][CH2:5]2.Cl.[CH3:14][O:15][NH2:16]>CO.O>[CH3:14][O:15][N:16]=[C:7]1[C:8]2[C:4](=[CH:3][C:2]([Cl:1])=[CH:10][C:9]=2[Cl:11])[CH2:5][CH2:6]1Participants
5
Reactant 2
Product 1
Reagents, catalysts & solvents 2
Procedure
To a soln. of 5,7-dichloro-1-indanone (0.34 mmol) in 2 mL MeOH was added O-methylhydroxylamine HCl (0.34 mmol). The reaction mixture was stirred at RT for 17 h and then heated to 50° C. for 24 h. The mixture was cooled to RT, diluted with water and extracted 3 times with EtOAc. The comb. org. layers were dried over MgSO4 and conc. in vacuo to give the desired product as white solid.
Workup
- temperatureheated to 50° C. for 24 h
- temperatureThe mixture was cooled to RT
- extractionextracted 3 times with EtOAc
- dry with materiallayers were dried over MgSO4 and conc. in vacuo
Sources & evidence
- ORD record
- ord-555ebfd57e634e3aa7a71221c7dc404a
- Source dataset
- uspto-grants-2016_07
- Patent number
- US09388197B2
Reaction notes
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